ClinGen Allele Registry
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Canonical Allele Identifier:
PA645429065
Gene: FANCE
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
223359
ClinVar RCV:
RCV000416904
RCV000649006
RCV003488462
ClinVar Variation:
221623
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_068741.1:p.Arg200Cys
CA3771446
NM_021922.3:c.598C>T